A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3517845



Internal ID18469440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46469867..46631445hg38UCSC Ensembl
Innerchr10:46918172..47079584hg19UCSC Ensembl
Innerchr10:46338178..46499590hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38161579
hg19161413
hg18161413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046194
Supporting Variants
Samples
Known GenesFAM35BP, GPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3517845
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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